Abstract  Density and isobaric heat capacity per unit volume were determined for aqueous mixtures of 1,2-ethanediol, 1,2-propanediol, 1,3-propanediol, 1,4-butanediol, and 1,2-hexanediol over the whole composition range in the temperature interval (283.15-313.15) K at atmospheric pressure. From these data, excess molar volumes and excess isobaric molar heat capacities were obtained. The comparison of experimental data with literature values shows quite good agreement, not only for absolute magnitudes, but also for excess quantities. Excess volumes are negative over the whole composition range and they become more ideal (less negative) as temperature increases. Excess isobaric molar heat capacity is mostly positive, although it is negative for some mixtures at several compositions and temperatures. Moreover, it was found that it presents a maximum at low mole fraction of the alcohol for most systems, as it was previously found for alkanol + water mixtures. As for temperature dependence, excess isobaric molar heat capacity increases with raising temperature in all cases. This increase is more pronounced for concentrated solutions of dialcohol, with the exception of the 1,2-hexanediol system. The obtained results are interpreted in terms of well-known arguments based on definition of excess magnitudes and chemical nature of the compounds. (C) 2013 Elsevier B.V. All rights reserved.

Abstract  Parabens are used as antimicrobial preservatives in consumer products. Exposure to methylparaben (MP) has been associated with adverse health outcomes, therefore, an alternative compound, 1,2-hexanediol (1,2-H), has been applied for cosmetics. In the present study, the phototoxicity of MP and 1,2-H, as well as the toxic effect caused by chronic exposure, were investigated using Daphnia magna. The 48 h acute toxicity tests with D. magna were conducted under indoor or ultraviolet (UV) light irradiation conditions, i.e., exposure to 4 h/d sunlight. Changes in the transcription of genes related to oxidative stress were determined in D. magna juveniles, to investigate the underlying mechanism of phototoxicity. The 21 d chronic toxicity tests of MP and 1,2-H were performed under indoor light irradiation. Exposure to MP under environmental level of UV light was more detrimental to D. magna. Transcripts of catalase and glutathione-S-transferase genes in D. magna was significantly increased by co-exposure to MP and UV light. After 21 d of chronic exposure to MP and 1,2-H, the reproduction no-observed effect concentrations for D. magna were 1 and >10 mg/L, respectively. The present study showed that exposure to UV could magnify the toxicity of MP on daphnids. Although acute and chronic toxicities of 1,2-H were generally lower than those of MP, its effects on other aquatic organisms should not be ignored. Further studies are needed to identify other mechanisms of MP phototoxicity.

Abstract  Atmospheric aerosol particles are often partially or completely composed of inorganic salts, such as ammonium sulfate and sodium chloride, and therefore exhibit hygroscopic properties. Many inorganic salts have well-defined deliquescence and efflorescence points at which they take up and lose water, respectively. Field measurements have shown that atmospheric aerosols are not typically pure inorganic salt, instead, they often also contain organic species. There is ample evidence from laboratory studies that suggests that mixed particles exist in a phase-separated state, with an aqueous inorganic core and organic shell. Although phase separation has not been measured in situ, there is no reason it would not also take place in the atmosphere. Here, we investigate the deliquescence and efflorescence points, phase separation and ability to exchange gas-phase components of mixed organic and inorganic aerosol using a flow tube coupled with FTIR (Fourier transform infrared) spectroscopy. Ammonium sulfate aerosol mixed with organic polyols with different O : C ratios, including 1,4-butanediol, glycerol, 1,2,6-hexanetriol, 1,2-hexanediol, and 1,5-pentanediol have been investigated. Those constituents correspond to materials found in the atmosphere in great abundance and, therefore, particles prepared in this study should mimic atmospheric mixed-phase aerosol particles. Some results of this study tend to be in agreement with previous microscopy experiments, but others, such as phase separation properties of 1,2,6-hexanetriol, do not agree with previous work. Because the particles studied in this experiment are of a smaller size than those used in microscopy studies, the discrepancies found could be a size-related effect.

Abstract  The objective of the present study is to investigate the effect of hydrocarbon chain length in 1,2-alkanediols on percutaneous absorption of metronidazole (MTZ). Twelve formulations (1,2-propanediol, 1,2-butanediol, 1,2-pentanediol, 1,2-hexanediol in 4% concentration, 1,2-hexanediol, and 1,2-heptanediol in 1% concentration, in the absence and presence of 1,4-cyclohexanediol, respectively) were studied in an in vitro hairless mouse skin model using Franz diffusion cell. Based on the flux values and retardation ratios (RR), a penetration retardation effect on percutaneous absorption of MTZ was observed for the formulations containing 1,2-diols having six- to seven-carbon chain in the presence of 1,4-cyclohexanediol (1,2-hexanediol with chain length of six hydrocarbons, RRs are 0.69 and 0.76 in the concentration of 4% and 1%, respectively; 1,2-heptanediol with chain length of seven hydrocarbons, RR is 0.78 in the concentration of 1%). On the other hand, no retardation effect was observed in formulations containing short alkyl chains (RRs of 1,2-propanediol, 1,2-butanediol, and 1,2-pentanediol are 0.99, 1.61, and 0.96, respectively). Instead, a penetration enhancement effect was observed for 1,2-diols having four and five carbons. In other words, effect of 1,2-alkanediols on percutaneous absorption of MTZ can be systematically modulated by simply varying number of -CH2 groups in the hydrocarbon chain-from being a penetration enhancer to retardant. These observations shed light on mechanism of the penetration enhancement and retardation effect and provide insight into rational design of penetration enhancers and retardants. Furthermore, the combination of 1,2-alkanediols and 1,4-cyclohexanediol could become a general vehicle for controlled release of pharmaceutical and cosmetic active ingredients.

Abstract  Caprylyl glycol and related 1,2-glycols are used mostly as skin and hair conditioning agents and viscosity agents in cosmetic products, and caprylyl glycol and pentylene glycol also function as cosmetic preservatives. The Cosmetic Ingredient Review (CIR) Expert Panel noted that, while these ingredients are dermally absorbed, modeling data predicted decreased skin penetration of longer chain 1,2-glycols. Because the negative oral toxicity data on shorter chain 1,2-glycols and genotoxicity data support the safety of the 1,2-glycols reviewed in this safety assessment, the Panel concluded that these ingredients are safe in the present practices of use and concentration described in this safety assessment.

Abstract  The micelle formation process for a typical anionic surfactant. sodium dodecyl sulfate, and a typical cationic surfactant, dodecyltrimethylammonium bromide, has been investigated in a series of mixed solvents consisting of different concentrations of isomeric hexanediols (1,2-hexanediol and 1,6-hexanediol) in water. The critical micelle concentrations and the degrees of counterion dissociation of the mixed micelles were obtained from conductance experiments. Luminescence probing experiments have been used to determine the concentration of micelles in solution and, hence, the micellar aggregation numbers of the surfactants in the mixed solvent systems. The alcohol aggregation numbers were determined by combining the partition coefficients (obtained using NMR paramagnetic relaxation enhancement experiments) with the micellar concentrations from the luminescence probing experiments. All these results are interpreted in terms of the difference in the interaction of the isomeric hexanediols with the surfactant as a function of the position of the hydroxyl groups on the six-carbon chain of the alcohol.

Abstract  Long chain aliphatic 1,2-diols like 1,2-hexanediol and 1,2-octanediol can be converted to the corresponding alpha-hydroxy-alkanoates with total chemoselectivity, in an oxidation catalyzed by an aqueous gold sol under O-2 atmosphere. The sol is stabilized with poly(vinylalcohol), and the reaction is performed in alcohol solvents. Two methods are proposed for the efficient recycling of the colloidal Au catalyst. Firstly a solvent-resistant membrane filtration can be applied. As the membrane material, poly(dimethylsiloxane) is chosen. Secondly, in appropriate conditions, the reaction proceeds in the liquid biphasic mode, and the aqueous Au sol can be recycled by phase separation. Using either of both approaches, the colloidal stability and catalytic activity can be preserved over several recycles.

Abstract  Background: Traditional preservation systems currently used in cosmetic and skin care products are safe and effective. New ingredients with similar efficacy are continually being introduced to fulfill this function. Objective: To study the potential for delayed type IV allergic hypersensitivity and irritation of a new preservative system containing 1,2-hexanediol and caprylyl glycol. Methods: A 200-subject repeat insult patch test (RIPT) was performed. A 15% mixture of 1,2-hexanediol and caprylyl glycol (equal parts of the two ingredients) in carbomer gel was placed under a series of 9 continuous occlusive induction patches, each 48 hours in duration. Three induction patches were applied each week, for a total of 3 weeks. Following a 10-day rest period during which no patches were applied, a single challenge application using the same mixture was applied and left on for 48 hours and read at 48 and 72 hours postapplication. A cosmetic formulation containing this same preservation system at an actual use concentration was tested by the same RIPT protocol. Results: Two hundred and twelve subjects completed the study. One hundred and sixty-eight were female and 44 were male ranging in age from 18 to 70 years. No reactions were seen during the induction or challenge phases. An additional 212 subjects were enrolled in a separate RIPT that evaluated the cosmetic formulation containing the same preservation system. No delayed type IV allergic hypersensitivity or irritation reactions were observed. Conclusion: A new preservative system utilizing 1,2-hexanediol and caprylyl glycol did not induce delayed type IV allergic hypersensitivity or irritation in human subjects.

Abstract  A study has been made of the acetoxylation of 1-hexene and cyclohexene in the presence of PdCl42- and a nitrate-iodate reoxidative system ensuring high yields of the corresponding acetoxyalkanes. It has been established that a binuclear pi-olefinic bridge-type palladium complex is a catalytically active particle. It is assumed that the mechanisms of formation of 1,2-hexanediol monoacetate and diacetoxycyclohexane differ at the final stage of transformation of the acetoxonium ion. Acetoxylation is retarded by the reaction products, which screen the coordination sphere of palladium.

Abstract  Aqueous dilute solutions of 2-butoxyethanol, 1,2-hexanediol, tert-butanol, 1-pentylamine and 1-butylamine are analized through the dynamic light scattering technique. The mutual diffusion coefficient is determined against amphiphile composition, showing, in all cases, clear minima in the dilute region. Using the Stokes-Einstein relation, the mean size of the aggregates is also obtained as a function of mole fraction. For enough concentrated solutions, structures in the range 2-20 angstrom are observed. It is found that both their size and the minimum amphiphile mole fraction for which aggregation is observed are strongly correlated with the hydrophobic character of the amphiphile. (C) 2017 Elsevier B.V. All rights reserved.

Abstract  We report the use of the ionic liquid tetrabutylphosphonium bromide as a solvent and catalyst for dehydration of diols to conjugated dienes. This system combines stability, high reaction rates, and easy product separation. A reaction mechanism for the model compound 1,2-hexanediol is proposed and experimentally corroborated. This particular mechanism allows for the selective formation of conjugated dienes, in contrast with purely acidic catalysis. Next, the reaction is also performed on various other diols. As a first application, we assessed the biobased production of 1,3-butadiene. With 1,4-butanediol as the starting material, a 94% yield of butadiene was reached at 100% conversion.

Abstract  Sorbitol can be selectively transformed into liquid alkanes over a bifunctional catalytic system Pt/ZrO2 + TiO2-WOx. In this paper, we investigated the reaction mechanism by carefully analyzing the numerous products issued from sorbitol and by studying the reactivity of some identified intermediates (1-hexanol 2-hexanol, 2-hexanone, 2,5-dimethyltetrahydrofuran, 1,2-hexanediol and 1,2,6-hexanetriol). This led us to propose that C-C cleavage reactions occur on terminal C-C bonds and mainly consist of dehydrogenation-decarbonylation reactions. The limiting steps of the sorbitol transformation are the isosorbide and mono-oxygenated intermediate transformations, especially the hydrogenation of ketones. It is also assessed that diols or triols with n carbon atoms are mainly converted in compounds with n - 1 carbon atoms. Short compounds (1 to 3 carbon atoms) are obtained via a dehydrogenation-retro-aldol reaction pathway and not from isosorbide conversion. (C) 2014 Elsevier Inc. All rights reserved.

Abstract  BACKGROUND/AIMS: The research on the treatment of "dry skin syndrome" is hampered by the lack of a suitable animal model. Formerly, we developed a validated guinea pig in vivo model in which the dry skin syndrome persists at least for 1 week. We can, therefore, compare the pharmacological effectiveness of known and potential moisturizers for the treatment of dry skin syndrome. Our aim is to study whether the moisturizing efficiency of humectants depends on the solvents in which they are dissolved.

METHODS: "Dry skin syndrome" was induced on the shaved skin on one side of guinea pigs by daily application of 2% sodium lauryl sulphate in deionized water (SLS) for 3 days. The other shaved side was used as control. After ascertaining skin dryness, that side was treated for 6 days with glycerol or 1,2-hexanediol in different solvents: water, or medium chain triglycerides (MCT) or mixtures of MCT with isopropyl alcohol in different proportions. Measurement of the in vivo moisturizing effect was carried out by a Comeometer CM 825; erythema was measured by a Mexameter MX 16.

RESULTS: Treatments with glycerol (1M) in water reversed the skin dryness shown by both instruments. When dissolving glycerol in MCT, no moisturizing effect was found, probably because glycerol does not dissolve in the oil. No moisturizing effect was found with different combinations of glycerol in the mixtures of MCT and isopropyl alcohol. No moisturizing effect was found using another polyol moisturizer: 1,2 hexanediol (1M) dissolved in MCT oil. Glycerol or 1,2-hexanediol abolished the erythema only when they were dissolved in water alone.

CONCLUSION: Polyol moisturizers such as glycerol or 1,2-hexanediol do not act in the presence of oils against the sodium lauryl sulphate-induced dry skin in our guinea pig model. Since in an oil-in-water (O/W) emulsion, the water evaporates within several minutes, one has to question the ability of moisturizing emulsions to treat dry skin. In such instances, one cannot draw conclusions about the moisturizing efficiency of the preparation merely from the presence of the humectant. One has to study the effect of the finished preparation.

Abstract  A series of novel pentacoordinated germanium(IV) complexes (I) has been prepared by the reaction of germanium dioxide with diols, such as 1,2-propanediol, 1,2-butanediol, 2,3-dimethyl-2,3-butanediol ,1-phenyl-1,2-ethanediol, 1,2-hexanediol, 3,3-dimethyl-1,2-butanediol in an aqueous sodium hydroxide medium. The general molecular formula can be represented as NaGe(OH)L2 where L is the deprotonated diol The reaction of germanium dioxide with catechol in distilled water gives Ge(C6H4O2)2.2H2O (II). Further treatment of this complex (II) with methanol, ethanol or 2-propanol gives hexacoordinated germanium (IV) complexes (III), Ge(C6H4O2)2.2ROH (where R = CH3, C2H5, (CH3)2CH, respectively). These complexes, which have been characterized by elemental analyses, thermogravimetric analyses, infrared, H-1 and C-13 NMR spectral studies, reveal that the pentacoordinated germanium(IV) complexes (I) have a slightly distorted trigonal-bipyramidal geometry. However, the suitable structure of the hexacoordinated complexes (II-III) are octahedral.

Abstract  The ceria-supported rhenium catalyst modified with palladium (ReOx-Pd/CeO2 (Re = 2 wt %, Pd/Re = 0.25)) is still the best catalyst for simultaneous hydrodeoxygenation. Higher Re loading amount decreased the activity. The simultaneous hydrodeoxygenation of cyclic vicinal diols occurs with high cis-stereoselectivity. ReOx-Pd/CeO2 catalysts were characterized by means of XRD, TEM, H-2-TPR, XAFS, XPS, Raman, and DFT calculations. The Re species on ReOx-Pd/CeO2 (Re = 2 wt %, Pd/Re = 0.25) catalyst after reduction and after stoichiometric reaction of 1,2-hexanediol to 1-hexene were Re-IV and Re-VI, and the Re-IV species were converted to Re-VI through the stoichiometric reaction. The Re species on ReOx-Pd/CeO2 are proposed to be randomly located on the CeO2 surface, and probably only monomeric Re species have catalytic activity for simultaneous hydrodeoxygenation. This model can explain the higher activity of Re = 2 wt % catalyst than those of higher Re loading catalysts. The reaction is proposed to proceed by the tetra/hexavalent redox cycle of the Re center in the catalysis followed by hydrogenation.

Abstract  Surface tension of aqueous solutions of 1,2-hexanediol (1,2HD), 1,5-hexanediol (1,5HD), 1,6-hexanediol (1,6HD), and 2,5-hexanediol (2,5HD) was measured as a function of composition using the method of capillary rise at 283.15, 288.15, 293.15, 298.15, 303.15 and 308.15 K with emphasis in the very dilute region.

The experimental data were used according to the model proposed by Connors for liquid solutes. Binding constants were determined for 1,2-hexanediol (1,2HD), 1,5-hexanediol (1,5HD) and 2,5-hexanediol (2,5HD). Infinite dilution activity coefficients were evaluated using the procedure suggested by Gracia-Fadrique and the results are discussed in terms of temperature and the size of the alkyl chain exposed to the solvent.

Pure 1,6-hexanediol (1,6HD) is a solid at the selected temperatures so the models mentioned before were not used with this solute.

The surface tension data, the binding constants and the infinite dilution activity coefficients were correlated with the position of hydroxyl groups in the solute and the results were used to evaluate the effect of hexanediols on the water structure. (c) 2007 Elsevier B.V. All rights reserved.

Abstract  Enantiospecific syntheses of methyl 2,3,4-trideoxy-alpha-D- and -beta-D-glycero-hexopyranoside (10 and 11), methyl-alpha-D- and beta-D-amicetopyranoside (24 and 25), (2S)-1,2-hexanediol (36), (2S)-1,2,6-hexanetriol (37), and some derivatives thereof from D-glucono-1,5-lactone are described.

Abstract  A green synthesis of silver nanoparticles was developed, using a low-toxic system of microemulsion and nano emulsion with castor oil as the oily phase, Brij 96 V and 1,2-hexanediol as the surfactant and co-surfactant respectively. Geranium (P. hortorum) leaf aqueous extract was employed as a reducing agent. The content and concentration of a metallic precursor and geranium leaf extract (GLE) in the systems used makes it possible to obtain different sizes of silver nanoparticles from 25 to 150 nm. The characterization by FTIR and Z potential shows that the biomolecules of the plant extract act as a reducing and capping agent, giving negative charges to the nanoparticle surface. The present study represents a contribution to the green synthesis of silver nano particles that can be extended to other metals.

Abstract  The purpose of this study was to develop tretinoin-loaded phospholipid vesicles, namely conventional liposomes, hexosomes, glycerosomes and ethosomes, and to investigate their efficacy on croton oil induced rosacea. Vesicles were prepared with soy phospholipid, sodium deoxycholate and tretinoin; 1,2-hexanediol, glycerol and ethanol were added to obtain hexosomes, glycerosomes and ethosomes, respectively. The prepared formulations were characterized in terms of size distribution, morphology, zeta potential and entrapment efficiency. All vesicles were spherical in shape with a mean diameter ranging between 60 and 132 nm and a fairly narrow distribution (0.23-0.29), negative zeta potential values (from -19 to -29 mV) and entrapment efficiency between 32 and 63%. Furthermore, vesicles were evaluated for an in vitro model of dermal delivery, and their mode of action was studied by performing confocal laser scanning microscopy (CLSM) and attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) analyses. In addition, in vivo skin penetration was also investigated. The results of in vitro and in vivo studies showed that vesicular formulations, especially hexosomes, promoted the drug deposition into the skin stratums and reduced the permeation into the blood. Finally, administration of vesicular tretinoin on croton oil-induced skin resulted in marked attenuation of oedema and inflammatory cells, especially using hexosomes. The proposed approach based on tretinoin vesicular formulations may be of value in the treatment of rosacea.

Abstract  n-Alkanol inhibition of N-methyl-D-aspartate (NMDA) receptors exhibits a "cutoff" effect: alcohols with up to eight to nine carbon atoms inhibit the receptor, whereas larger alcohols do not. This phenomenon was originally proposed to result from size exclusion; i.e., alcohols above the cutoff are too large to bind to an amphiphilic site on the receptor. In the present study, 1,Omega-diols with 3 to 14 carbon atoms inhibited NMDA-activated current in Chinese hamster ovary and human embryonic kidney 293 cells transiently expressing NR1 and NR2B NMDA receptor subunits. Results of fluctuation analysis experiments were consistent with a similar mechanism of inhibition of NMDA-activated current by alcohols and diols. The average change in apparent energy of binding of the diols caused by addition of a methylene group was 2.1 kJ/mol, which is consistent with an important role of hydrophobic interactions. Because 1,Omega-diols with 9 to 14 carbons inhibited NMDA-activated current, despite having molecular volumes exceeding that at the cutoff point for 1-alkanols, a size exclusion mechanism seems inadequate to explain the cutoff effect. A disparity in hydrophobicity values at the cutoff for alcohols and diols, however, revealed that hydrophobicity could also not entirely explain the cutoff phenomenon. From these results, it seems that the cutoff effect on NMDA receptors results primarily from the inability of long-chain alcohols to achieve adequate concentrations at their site of action due to low aqueous solubility, although other factors may also contribute to the effect.

Abstract  During the recovery of recombinant proteins from gram negative bacteria, many of the methods used to extract proteins from cells release lipopolysaccharides (LPS, endotoxin) along with the protein of interest. In many instances, LPS will co-purify with the target protein due to specific or non-specific protein-LPS interactions. We have investigated the ability of alkanediols to effect the separation of LPS from protein-LPS complexes while the complexes are immobilized on ion exchange chromatographic resins. Proteins were complexed with fluorescently labeled LPS and bound to ion exchange resin. Alkanediol washes of the resins were preformed and the proteins eluted. Column eluates were monitored for LPS and protein by fluorescence and UV spectroscopy, respectively. Alkanediols were effective agents for dissociating LPS from protein-LPS complexes. The efficiency of LPS removal increased with increasing alkanediol chain length. The 1,2-alkanediol isomers were more effective than terminal alkanediol isomers in the separation of LPS from protein-LPS complexes, while the separation of LPS from protein-LPS complexes was more efficient on cation exchangers than on anion exchangers. In addition, it was noted during these investigations that the 1,2-alkanediols increased the retention time of the proteins on the ion exchange resins. Alkanediols provide a safer alternative to the use of other organics such as alcohols or acetonitrile for the separation of LPS from protein due to their lower toxicity and decreased inflammability. In addition, they are less costly than many of the detergents that have been used for similar purposes.